Rat Platelet Activating Factor (PAF) ELISA Kit PAF Instructions
December 10 11:18:53, 2020
Rat Platelet Activating Factor (PAF) ELISA Kit User Manual Xiamen Huijia Biotechnology Co., Ltd. This kit is for research use only. Detection range: 0.23 ng / ml-15 ng / ml Minimum detection limit: 0.1 ng / ml Specificity: This kit can detect natural or recombinant rat PAF at the same time, and does not cross-react with other related proteins. Validity: 6 months Expected application: ELISA method for quantitative determination of PAF content in rat serum, plasma, cell culture supernatant or other related biological fluids. Description 1. Kit storage: -20 ℃ (when not in use for a long time); 2-8 ℃ (when used frequently). 2. The concentrated washing liquid will be salted out at low temperature, and it can be heated and dissolved in the water bath when diluted. 3. There may be inconsistencies between the Chinese and English instructions. Please refer to the English instructions. 4. The well of the ELISA plate just opened may contain a little water-like substance. This is normal and will not have any impact on the experimental results. Experimental principle The microtiter plate is coated with purified antibody to make a solid phase carrier, and the specimen or standard, biotinylated anti-PAF antibody, and HRP-labeled avidin are sequentially added to the microwell coated with anti-PAF antibody After thorough washing, the color is developed with the substrate TMB. TMB is converted into blue under the catalysis of peroxidase, and into the final yellow under the action of acid. The color depth is positively correlated with the PAF in the sample. The absorbance (OD value) was measured with a microplate reader at a wavelength of 450 nm, and the sample concentration was calculated. Kit composition and reagent preparation enzyme-linked plate (Assay plate): one piece (96 wells). Standard product (Standard): 2 bottles (lyophilized product). Sample Diluent: 1 × 20ml / bottle. Biotin-antibody Diluent: 1 × 10ml / bottle. Horseradish peroxidase labeled avidin diluent? (HRP-avidin Diluent): 1 × 10ml / bottle. Biotin-antibody: 1 × 120μl / vial (1: 100) Horseradish peroxidase-labeled avidin (HRP-avidin): 1 × 120μl / vial (1: 100) Substrate solution ( TMB Substrate): 1 × 10ml / bottle. Wash Buffer: 1 × 20ml / bottle, each bottle is diluted 25 times with distilled water. Stop solution (Stop Solution): 1 × 10ml / bottle (2N H2SO4). Reagents and equipment that are not provided are standard specifications, microplate readers, high-speed centrifugal electromechanical thermostatic incubators, clean test tubes and Eppendof tube series adjustable pipettes and tips. It is best to use multi-channel pipettes when there are many samples at one time. 6. Distilled water, volumetric flasks and other specimen collection and storage of serum: Whole blood specimens should be placed at room temperature for 2 hours or 4 ℃ overnight after centrifugation at 1000g for 20 minutes, take the supernatant for detection, or put the specimen at -20 ℃ or Store at -80 ℃, but avoid repeated freezing and thawing. Plasma: EDTA or heparin can be used as an anticoagulant. Centrifuge the sample at 1000g at 2-8 ° C for 15 minutes within 30 minutes after collection, or store the specimen at -20 ℃ or -80 ℃, but avoid repeated freezing and thawing. Cell culture supernatant or other biological specimens: centrifuge at 1000g for 20 minutes, take the supernatant for detection, or store the specimen at -20 ℃ or -80 ℃, but avoid repeated freezing and thawing. Note: Hemolysis of specimens will affect the final test results, so hemolysis specimens should not be tested. Dilution principle of the specimen: firstly, the approximate content of the sample to be tested is determined through literature search, and the appropriate dilution factor is determined. Only when it is diluted to the range of the standard curve, the test result is accurate. Detailed records should be made during the dilution process. When calculating the concentration at the end, it was diluted "N" times, and the concentration of the specimen should be multiplied by "N". Standard dilution principle: 2 bottles, each bottle is diluted to 1ml with sample diluent before use, and then left to stand for more than 10 minutes after being capped, and then inverted / rubbed repeatedly to help dissolve. Its concentration is 15 ng / ml. After serial dilutions, they are diluted 15 ng / ml, 7.5 ng / ml, 3.75 ng / ml, 1.87 ng / ml, 0.94 ng / ml, 0.47 ng / ml, 0.23 ng / ml, and the sample dilution is directly used as the standard concentration 0 ng / ml, prepared within 15 minutes before use. If preparing 7.5 ng / ml standard: take 0.5ml (not less than 0.5ml) of the above standard at 15 ng / ml and add it to the Eppendorf tube containing 0.5ml of sample diluent, mix well, and the rest of the concentration can be deduced by analogy. Dilution principle of biotin-labeled antibody: before use, dilute with biotin-labeled antibody diluent. Before dilution, prepare according to the pre-calculated total amount required for each experiment (100 μl per well). In actual preparation, 0.1- 0.2ml. For example, 10 μl of biotin-labeled antibody plus 990 μl of biotin-labeled antibody dilution is prepared, mixed gently, and prepared within one hour before use. Dilution principle of horseradish peroxidase-labeled avidin: before use, dilute with horseradish peroxidase-labeled avidin diluent, and prepare according to the pre-calculated total amount required for each experiment before dilution (Each 100μl), 0.1-0.2ml should be prepared in actual preparation. For example, 10μl horseradish peroxidase-labeled avidin plus 990μl horseradish peroxidase-labeled avidin diluent is prepared in the ratio, gently mixed, and prepared within one hour before use. Before starting the experiment, please configure all reagents in advance. When diluting the reagents or samples, they should be mixed evenly. Try to avoid foaming when mixing. A standard curve should be made for each test. If the sample concentration is too high, dilute with sample diluent to make the sample meet the detection range of the kit. Sample adding: set blank hole, standard hole and sample hole to be tested. Add 100μl of sample diluent to blank wells, and add 100μl of standard or test sample to the remaining wells. Be careful not to have air bubbles. Add the sample to the bottom of the well of the microtiter plate, try not to touch the wall of the well, gently shake to mix, enzyme The target plate is covered with a cover or film and reacted at 37 ° C for 120 minutes. To ensure the validity of the experimental results, please use a new standard solution for each experiment. Discard the liquid and spin dry without washing. Add 100μl of biotinylated antibody working solution to each well (proportion of 1μl of biotinylated antibody plus 99μl of biotinylated antibody dilution), mix gently and prepare within one hour before use), 37 ℃, 60 minutes. After incubating for 60 minutes, discard the liquid in the wells, spin dry, wash the plate 3 times, soak for 1-2 minutes each time, 200 μl / well, spin dry. Add 100 μl of horseradish peroxidase-labeled avidin working solution (with biotin-labeled antibody working solution) to each well at 37 ° C for 60 minutes. After incubating for 60 minutes, the liquid in the wells was discarded, spin-dried, and the plate was washed 5 times, soaking for 1-2 minutes each time, 200 μl / well, and dried. Add 90μl of substrate solution to each well in sequence, and develop color at 37 ℃ in the dark. To terminate). Add 50μl of stop solution to each well in sequence to stop the reaction (in this case, the blue color turns to yellow). The order of adding the stop solution should be the same as that of the substrate solution. In order to ensure the accuracy of the experimental results, the termination solution should be added as soon as possible after the substrate reaction time expires. The optical density (OD value) of each well was measured sequentially with an enzyme-linked instrument at a wavelength of 450 nm. Test within 15 minutes after adding stop solution. Note: 1. When using the kit for the first time, the user should centrifuge various reagent tubes for a few minutes so that the reagents are concentrated to the bottom of the tube. 2. Leave one well for each experiment as a blank zero-adjusting well. No reagents are added to this well, but the substrate solution and 2N H2SO4 are added last. Use this hole to adjust the OD value to zero when measuring. 3. To prevent the sample from evaporating, place the reaction plate in a closed box covered with a damp cloth during the test, and add a cover or film to the enzyme label plate. 4. Store unused microplates or reagents at 2-8 ° C. Standards, biotin-labeled antibody working solution, horseradish peroxidase-labeled avidin working solution, please use according to the required amount. Do not reuse diluted standard, biotin-labeled antibody working solution, or horseradish peroxidase-labeled avidin working solution. 5. It is recommended to set double-hole measurement when testing samples to ensure the accuracy of the test results. Plate washing method Manual plate washing method: suck (do not touch the wall) or shake off the liquid in the microplate; place a few layers of absorbent paper on the experimental table, and force the microplate down several times; pat the recommended wash buffer Inject at least 0.3ml of solution into the hole and soak for 1-2 minutes. Repeat this process several times as needed. Automatic plate washing: If there is an automatic plate washing machine, it should be used in the formal experiment process after being used skillfully. Calculate the standard concentration as the abscissa (logarithmic coordinate), the OD value is the ordinate (ordinary coordinate), draw a standard curve on semi-logarithmic coordinate paper, and find the corresponding concentration from the standard curve according to the OD value of the sample ; Multiply by the dilution factor; or use the standard concentration and OD value to calculate the linear regression equation of the standard curve, substitute the OD value of the sample into the equation, calculate the sample concentration, and multiply by the dilution factor, which is the actual concentration of the sample . Matters needing attention 1. When mixing protein solution should be as gentle as possible to avoid foaming. 2. The washing process is very important. Insufficient washing can easily cause false positives. 3. It is best to control the sampling time within 5 minutes. If there are many specimens, it is recommended to use a volley gun to add samples. 4. Please make the standard curve at the same time of each measurement, it is better to make the complex hole. 5. If the content of the substance to be tested in the specimen is too high, please dilute it and then determine it. When calculating, please multiply by the dilution factor. 6. When preparing standard products and testing solution working fluid, please prepare with corresponding diluent, not to be confused. 7. Please keep the substrate away from light. 8. Do not replace the reagents in the kit with reagents from other manufacturers.
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